1vs6

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(New page: 200px<br /><applet load="1vs6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1vs6, resolution 3.46&Aring;" /> '''Crystal structure of...)
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[[Image:1vs6.gif|left|200px]]<br /><applet load="1vs6" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1vs6, resolution 3.46&Aring;" />
caption="1vs6, resolution 3.46&Aring;" />
'''Crystal structure of the bacterial ribosome from escherichia coli in complex with the antibiotic kasugamyin at 3.5A resolution. this file contains the 50s subunit of one 70s ribosome. the entire crystal structure contains two 70s ribosomes and is described in remark 400.'''<br />
'''Crystal structure of the bacterial ribosome from escherichia coli in complex with the antibiotic kasugamyin at 3.5A resolution. this file contains the 50s subunit of one 70s ribosome. the entire crystal structure contains two 70s ribosomes and is described in remark 400.'''<br />
==Overview==
==Overview==
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The prokaryotic ribosome is an important target of antibiotic action. We, determined the X-ray structure of the aminoglycoside kasugamycin (Ksg) in, complex with the Escherichia coli 70S ribosome at 3.5-A resolution. The, structure reveals that the drug binds within the messenger RNA channel of, the 30S subunit between the universally conserved G926 and A794, nucleotides in 16S ribosomal RNA, which are sites of Ksg resistance. To, our surprise, Ksg resistance mutations do not inhibit binding of the drug, to the ribosome. The present structural and biochemical results indicate, that inhibition by Ksg and Ksg resistance are closely linked to the, structure of the mRNA at the junction of the peptidyl-tRNA and exit-tRNA, sites (P and E sites).
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The prokaryotic ribosome is an important target of antibiotic action. We determined the X-ray structure of the aminoglycoside kasugamycin (Ksg) in complex with the Escherichia coli 70S ribosome at 3.5-A resolution. The structure reveals that the drug binds within the messenger RNA channel of the 30S subunit between the universally conserved G926 and A794 nucleotides in 16S ribosomal RNA, which are sites of Ksg resistance. To our surprise, Ksg resistance mutations do not inhibit binding of the drug to the ribosome. The present structural and biochemical results indicate that inhibition by Ksg and Ksg resistance are closely linked to the structure of the mRNA at the junction of the peptidyl-tRNA and exit-tRNA sites (P and E sites).
==About this Structure==
==About this Structure==
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1VS6 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with MG as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1VS6 OCA].
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1VS6 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=MG:'>MG</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1VS6 OCA].
==Reference==
==Reference==
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[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Cate, J.H.D.]]
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[[Category: Cate, J H.D.]]
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[[Category: Schuwirth, B.S.]]
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[[Category: Schuwirth, B S.]]
[[Category: Vila-Sanjurjo, A.]]
[[Category: Vila-Sanjurjo, A.]]
[[Category: MG]]
[[Category: MG]]
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[[Category: ribosome]]
[[Category: ribosome]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 05:06:16 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:38:04 2008''

Revision as of 13:38, 21 February 2008


1vs6, resolution 3.46Å

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Crystal structure of the bacterial ribosome from escherichia coli in complex with the antibiotic kasugamyin at 3.5A resolution. this file contains the 50s subunit of one 70s ribosome. the entire crystal structure contains two 70s ribosomes and is described in remark 400.

Overview

The prokaryotic ribosome is an important target of antibiotic action. We determined the X-ray structure of the aminoglycoside kasugamycin (Ksg) in complex with the Escherichia coli 70S ribosome at 3.5-A resolution. The structure reveals that the drug binds within the messenger RNA channel of the 30S subunit between the universally conserved G926 and A794 nucleotides in 16S ribosomal RNA, which are sites of Ksg resistance. To our surprise, Ksg resistance mutations do not inhibit binding of the drug to the ribosome. The present structural and biochemical results indicate that inhibition by Ksg and Ksg resistance are closely linked to the structure of the mRNA at the junction of the peptidyl-tRNA and exit-tRNA sites (P and E sites).

About this Structure

1VS6 is a Protein complex structure of sequences from Escherichia coli with as ligand. Full crystallographic information is available from OCA.

Reference

Structural analysis of kasugamycin inhibition of translation., Schuwirth BS, Day JM, Hau CW, Janssen GR, Dahlberg AE, Cate JH, Vila-Sanjurjo A, Nat Struct Mol Biol. 2006 Oct;13(10):879-86. Epub 2006 Sep 24. PMID:16998486

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